ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10713318
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.5647756C>T
GRCh37
chr1:g.5707816C>T
Linked Data - Sequence & Population
gnomAD v2:
1:5707816 C / T
gnomAD v3:
1:5647756 C / T
gnomAD v4:
chr1-5647756-C-T
Joint Max Group AF
0.60851795 (AFR)
Genomes Max Group AF
0.60851795 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4845812
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.5647756C>T , CM000663.2:g.5647756C>T
GRCh38
NC_000001.10:g.5707816C>T , CM000663.1:g.5707816C>T
GRCh37
NC_000001.9:g.5630403C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'